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3
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0002691441
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[3] (a) T. Hayashi, M. Fukushima, M. Konishi and M. Kumada, Tetrahedron Lett., 21 (1980) 79;
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Hayashi, T.1
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4
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37049076815
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(b) T. Hayashi, A. Yamamoto, M. Hojo and Y. Ito, J. Chem. Soc., Chem. Commun., (1989) 495.
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5
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[4] T. Hayashi, K. Hayashizaki, T. Kiyoi and Y. Ito, J. Am. Chem. Soc., 110 (1988) 8153.
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Hayashi, T.1
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Ito, Y.4
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6
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0025820931
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[5] Cf. P-P ligands: (a) M. Yamagucchi, T. Shima, T. Yamagishi and M. Hida, Tetrahedron: Asymm., 2 (1991) 663;
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Yamagucchi, M.1
Shima, T.2
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Hida, M.4
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7
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0000345787
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(b) A. Togni, C. Breutel, A. Schnyder, F. Spindler, H. Landert and A. Tijani, J. Am. Chem. Soc., 116 (1994) 4062.
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Schnyder, A.3
Spindler, F.4
Landert, H.5
Tijani, A.6
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8
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0026588815
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N-N ligands: (c) U. Leutenegger, G. Umbricht, C. Fahrni, P. von Matt and A. Pfaltz, Tetrahedron, 48 (1992) 2143;
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Leutenegger, U.1
Umbricht, G.2
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Von Matt, P.4
Pfaltz, A.5
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10
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0028272321
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(e) D. Tanner, P.G. Andersson, A. Harden and P. Somfai, Tetrahedron Lett., 35 (1994) 4631;
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Tanner, D.1
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Somfai, P.4
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11
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0029051258
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(f) P. Gamez, B. Dunjic, F. Fache and M. Lemaire, Tetrahedron: Asymm., 6 (1995) 1109.
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Gamez, P.1
Dunjic, B.2
Fache, F.3
Lemaire, M.4
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12
-
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0027196559
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P-N ligands: (g) G.J. Dawson, C.G. Frost, J.M.J. Williams and S.J. Coote, Tetrahedron Lett., 34 (1993) 3149;
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Dawson, G.J.1
Frost, C.G.2
Williams, J.M.J.3
Coote, S.J.4
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16
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(k) J. Sprinz, M. Kiefer, G. Helmchen, M. Reggelin, G. Huttner, O. Walter and L. Zsolnai, Tetrahedron Lett., 35 (1994) 1523;
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Huttner, G.5
Walter, O.6
Zsolnai, L.7
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22
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33847087368
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(c) cf. R.B. Kress, E.N. Duesler, M.C. Etter, I.C. Paul and D.Y. Curtin, J. Am. Chem. Soc., 102 (1980) 7709.
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Curtin, D.Y.5
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24
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0001717911
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[8] (a) T. Hayashi, M. Konishi, M. Fukushima, T. Mise, M. Kagotani, M. Tajika and M. Kumada, J. Am. Chem. Soc., 104 (1982) 180;
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[9] (a) G. Consiglio, O. Piccolo, L. Roncetti and F. Morandini, Tetrahedron, 42 (1986) 2043;
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33
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0011564305
-
-
5k
-
(d) [5k];
-
-
-
-
38
-
-
0011691452
-
-
Highest asymmetric inductions reported: (E)-pent-3-ene-2-yl acetate, 97% e.e. [5i]; 3-acetoxy-cyclohexene, 96% e.e. [5j]
-
[13] Highest asymmetric inductions reported: (E)-pent-3-ene-2-yl acetate, 97% e.e. [5i]; 3-acetoxy-cyclohexene, 96% e.e. [5j].
-
-
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39
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0001277585
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[14] (a) K. Tamao, Y. Kiso, K. Sumitani and M. Kumada, J. Am. Chem. Soc., 94 (1972) 9268;
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41
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0011561790
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Molecular modelling experiments were performed on a Silicon Graphics Workstation using the program SYBYL (Trypos) version 6.2; details will be published elsewhere
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[15] Molecular modelling experiments were performed on a Silicon Graphics Workstation using the program SYBYL (Trypos) version 6.2; details will be published elsewhere.
-
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44
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0028209777
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[18] P. von Matt, O. Loiseleur, G. Koch, A. Pfaltz, C. Lefeber, T. Feucht and G. Helmchen, Tetrahedron: Asymm., 5 (1994) 573.
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Von Matt, P.1
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Koch, G.3
Pfaltz, A.4
Lefeber, C.5
Feucht, T.6
Helmchen, G.7
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46
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-
0011561791
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10b
-
(b) [10b].
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47
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0011572576
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Thesis, Regensburg
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[20] H.-J. Lautenschlager, Thesis, Regensburg, 1989.
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(1989)
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48
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[21] H. Brunner, H.-J. Lautenschlager, W.A. König and R. Krebber, Chem. Ber., 123 (1990) 847.
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50
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0011566179
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2
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2.
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51
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0004150157
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Siemens Crystallographic Research Systems
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[24] (a) G.M. Sheldrick, SHELXTL-PC, Release 4.1, Siemens Crystallographic Research Systems, 1990;
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(1990)
SHELXTL-PC, Release 4.1
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Sheldrick, G.M.1
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53
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0011567740
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Supplementary data (bond length, bond angles, torsional angles and structure factors) have been deposited at the Cambridge Crystallographic Data Centre
-
[25] Supplementary data (bond length, bond angles, torsional angles and structure factors) have been deposited at the Cambridge Crystallographic Data Centre.
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